Chahine M - Search Results

1

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes.

Baroudi G, Chahine M. Baroudi G, et al. Among authors: chahine m. FEBS Lett. 2000 Dec 29;487(2):224-8. doi: 10.1016/s0014-5793(00)02360-7. FEBS Lett. 2000. PMID: 11150514 Free article.

2

Restoration of fast inactivation in an inactivation-defective human heart sodium channel by the cysteine modifying reagent benzyl-MTS: analysis of IFM-ICM mutation.

Chahine M, Deschênes I, Trottier E, Chen LQ, Kallen RG. Chahine M, et al. Biochem Biophys Res Commun. 1997 Apr 28;233(3):606-10. doi: 10.1006/bbrc.1997.6510. Biochem Biophys Res Commun. 1997. PMID: 9168898 Free article.

3

Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage-gated sodium channels.

Chahine M, George AL Jr. Chahine M, et al. FEBS Lett. 1997 Aug 4;412(3):621-4. doi: 10.1016/s0014-5793(97)00869-7. FEBS Lett. 1997. PMID: 9276478 Free article.

4

Electrophysiological study of chimeric sodium channels from heart and skeletal muscle.

Deschênes I, Chen L, Kallen RG, Chahine M. Deschênes I, et al. Among authors: chahine m. J Membr Biol. 1998 Jul 1;164(1):25-34. doi: 10.1007/s002329900390. J Membr Biol. 1998. PMID: 9636241

5

SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells.

Baroudi G, Carbonneau E, Pouliot V, Chahine M. Baroudi G, et al. Among authors: chahine m. FEBS Lett. 2000 Feb 4;467(1):12-6. doi: 10.1016/s0014-5793(00)01099-1. FEBS Lett. 2000. PMID: 10664447 Free article.

6

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.

Deschênes I, Baroudi G, Berthet M, Barde I, Chalvidan T, Denjoy I, Guicheney P, Chahine M. Deschênes I, et al. Among authors: chahine m. Cardiovasc Res. 2000 Apr;46(1):55-65. doi: 10.1016/s0008-6363(00)00006-7. Cardiovasc Res. 2000. PMID: 10727653

7

The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family.

St-Pierre J, Roy N, Blier L, Plante E, Cote JM, Gilbert M, Chahine M. St-Pierre J, et al. Among authors: chahine m. Can J Cardiol. 2000 Mar;16(3):307-12. Can J Cardiol. 2000. PMID: 10744792

8

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

Baroudi G, Pouliot V, Denjoy I, Guicheney P, Shrier A, Chahine M. Baroudi G, et al. Among authors: chahine m. Circ Res. 2001 Jun 22;88(12):E78-83. doi: 10.1161/hh1201.093270. Circ Res. 2001. PMID: 11420310

9

Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.

Lupoglazoff JM, Cheav T, Baroudi G, Berthet M, Denjoy I, Cauchemez B, Extramiana F, Chahine M, Guicheney P. Lupoglazoff JM, et al. Among authors: chahine m. Circ Res. 2001 Jul 20;89(2):E16-21. doi: 10.1161/hh1401.095087. Circ Res. 2001. PMID: 11463728

10

Implication of the C-terminal region of the alpha-subunit of voltage-gated sodium channels in fast inactivation.

Deschênes I, Trottier E, Chahine M. Deschênes I, et al. Among authors: chahine m. J Membr Biol. 2001 Sep 15;183(2):103-14. doi: 10.1007/s00232-001-0058-5. J Membr Biol. 2001. PMID: 11562792

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